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IFI16 is a Periodontitis Modulating Protein (IFI)

Primary Purpose

Severe Periodontitis, Acute Inflammatory Response

Status

Completed

Phase

Not Applicable

Locations

United States

Study Type

Interventional

Intervention

Customized acrylic mouthguard

About this trial

This is an interventional basic science trial for Severe Periodontitis focused on measuring Teeth, Periodontal disease, acute inflammatory response, stent-induced biofilm overgrowth, periodontal pathogens

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Subjects must have read, understood and signed an informed consent form.
Subjects must be able and willing to follow study procedures and instructions.
Subjects must be adult males or females with a minimum of 18 years (inclusive).
Subjects must present with at least 20 teeth in the functional dentition, excluding third molars.
Subjects must have at least 3 teeth in each posterior sextant
Subjects must be in good general health
Subjects must be in the healthy (PPC-A) or severe periodontitis (PPC-G) categories according to the PPC (1)

Exclusion Criteria:

If the sextants identified for the analysis has implants
All individuals who meet criteria for anti-infective prophylaxis prior to dental procedures
Chronic disease with oral manifestations including diabetes mellitus.
Current smoker or one that has stopped smoking less than 2 years prior to enrollment.
Gross oral pathology other than the periodontal disease.
Treatment with antibiotics for any medical or dental condition within 1 month prior to the screening examination.
Chronic treatment (i.e., two weeks or more) with any medication known to affect periodontal status (e.g., phenytoin, calcium antagonists, cyclosporin, coumadin, non-steroidal anti-inflammatory drugs, aspirin) within one month of the screening examination.
Ongoing medications initiated less than three months prior to enrollment (i.e., medications for chronic medical conditions must be initiated at least three months prior to enrollment).
Significant organ disease including impaired renal function, heart murmur, history of rheumatic fever or valvular disease, or any bleeding disorder.
Individuals with prosthetic material used for intra-cardiac repair (e.g. for congenital heart disease), or intra-cardiac devices, cardiac transplant, infective endocarditis and individuals who have had previous infectious complications of prosthetic joint infections
Infectious diseases such as hepatitis, HIV or tuberculosis.
Anemia or other blood dyscrasias.
Anticoagulant therapy or drugs, such as heparin or warfarin.
Severe unrestored caries, or any condition that is likely to require antibiotic treatment over the trial.
Pregnant, or expect to become pregnant within the next several months.
Females of child-bearing capacity must be willing to have pregnancy test to confirm they are not pregnant.
Females of child-bearing capacity not using any form of contraceptive methods
Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.

Sites / Locations

University of North Carolina at Chapel Hill

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Arm Label

Periodontal Profile Class (PPC-A)

Periodontal Profile Class (PPC-G)

Arm Description

Periodontally healthy participants (PPC-A) will wear customized acrylic mouthguard only during tooth brushing for 21 days.

Participants with severe periodontal disease (PPC-G) will wear customized acrylic mouthguard only during tooth brushing for 21 days.

Outcomes

Primary Outcome Measures

Mean AIM2 mRNA fold change

Mean IFI16 mRNA fold change

Percentage of SIBO-induced AIM2 positive cells

Percentage of SIBO-induced IIFI16 M2 positive cells

Secondary Outcome Measures

Percent periodontal pathogens by expression of AIM2 and IFI16

Full Information

NCT ID

NCT03513497

First Posted

April 19, 2018

Last Updated

July 10, 2023

Sponsor

University of North Carolina, Chapel Hill

Collaborators

National Institute of Dental and Craniofacial Research (NIDCR)

1. Study Identification

Unique Protocol Identification Number

NCT03513497

Brief Title

IFI16 is a Periodontitis Modulating Protein

Acronym

IFI

Official Title

IFI16 is a Periodontitis Modulating Protein

Study Type

Interventional

2. Study Status

Record Verification Date

June 2023

Overall Recruitment Status

Completed

Study Start Date

October 18, 2018 (Actual)

Primary Completion Date

June 28, 2023 (Actual)

Study Completion Date

June 28, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

University of North Carolina, Chapel Hill

Collaborators

National Institute of Dental and Craniofacial Research (NIDCR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

To characterize the expression of IFI16 and AIM2 in gingival tissues in an inflammatory response using an acrylic mouthguard (also referred to as a stent) induced bacteria overgrowth method. Participants: A maximum of 72 Adult subjects will be recruited from the patients, students and staff at the University of North Carolina, as well as the general population in or near Chapel Hill NC. Procedures (methods): Medical history, demographics, (height/weight), urine based pregnancy test, vital signs (to include blood pressures, and pulse) standard dental clinical measures (to include plaque index, gingival index, bleeding on probing, and clinical attachment level), alginate impressions taken for fabrication of an acrylic stent (mouthguard), 2 gingival biopsies, 2 subgingival (below the gumline) plaque samples, and Scaling Root planing (SRP)/or adult prophylaxis

Detailed Description

A total of 72 subjects will be enrolled. Specifically, a sufficient number of adults 18 years and older will be screened until 36 healthy (PPC-A) subjects and 36 subjects with severe periodontal disease (PPC-G) will be enrolled. Eligibility for study participation will be determined during the screening session. Barring dropout, subject participation will include 1 to 8 visits lasting over a maximum period of 42 days. The last 3 visits (visit 5-8) will depend on the individual need of the subject for providing SRP. Clinical data and medical history data will be collected at the screening visit to ascertain eligibility. All subjects will have dental plaque and a gingival biopsy collected at baseline. Enrolled subjects will be included in an experimental gingivitis model Stent-Induced Biofilm Overgrowth (SIBO) for 21 days. Individuals will return for safety checks every week during the 21-day period. At 21-days, plaque samples and a gingival biopsy will be collected. For diseased individuals SRP will initiate during the 21-day visit at the SIBO quadrant. Visit 6 (28 days) will include the post-biopsy follow up, prophylaxis (for healthy individuals) and SRP (diseased individuals). Subjects receiving SRP may have 2 additional visits (visit 7 at day 35 and visit 8 at day 42) for completing the SRP of all quadrants and will be dependent on individual need. Medical histories, demographics, height and weight, clinical and biological data described above will be recorded and stored on a secure server located at the University of North Carolina. Each participant enrolled into the study will have a unique identification number that has been stripped of any information that could be used by non-study members to identify the subject.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Severe Periodontitis, Acute Inflammatory Response

Keywords

Teeth, Periodontal disease, acute inflammatory response, stent-induced biofilm overgrowth, periodontal pathogens

7. Study Design

Primary Purpose

Basic Science

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Masking

None (Open Label)

Allocation

Non-Randomized

Enrollment

72 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Periodontal Profile Class (PPC-A)

Arm Type

Experimental

Arm Description

Periodontally healthy participants (PPC-A) will wear customized acrylic mouthguard only during tooth brushing for 21 days.

Arm Title

Periodontal Profile Class (PPC-G)

Arm Type

Experimental

Arm Description

Participants with severe periodontal disease (PPC-G) will wear customized acrylic mouthguard only during tooth brushing for 21 days.

Intervention Type

Other

Intervention Name(s)

Customized acrylic mouthguard

Other Intervention Name(s)

intraoral stent

Intervention Description

Customized acrylic mouthguards extended to cover approximately 2 mm over gingival margins will be fabricated for each subject. Stents will form a seal and rest on the gingiva, but will be relieved on the tooth and tissue side except for the occlusal surfaces to avoid disturbing plaque or gingival tissues. Acrylic stents will cover the area in one sextant where no brushing and flossing teeth is to occur for 21 days.

Primary Outcome Measure Information:

Title

Mean AIM2 mRNA fold change

Time Frame